michael s
(Michael S)
#1
61 What drugs do post-transplant patients require,
and what are their side effects? How should I
follow up such patients?
Brendan Madden
Following successful cardiac, cardiopulmonary or pulmonary
transplantation, patients require life-long immunosuppressive
therapy. Routine immunosuppression consists of cyclosporin-A
and azathioprine, occasionally supplemented by cortico-
steroids. Episodes of acute allograft rejection are treated with
intravenous methylprednisolone therapy or occasionally anti-
thymocyte globulin or OKT3. Other drugs used include
tacrolimus, mycophenolate mofetil and cyclophosphamide.
Early evidence suggests that mycophenolate mofetil (an
antimetabolite drug) may be a useful alternative to azathioprine
as maintenance postoperative immunosuppression. OKT3 is a
monoclonal antibody raised in mice, which is directed against
the lymphocyte CD3 complex. Although it is sometimes used
for induction following transplantation it is now more
frequently employed in the management of severe episodes of
acute cardiac rejection.
Common complications following transplantation include
allograft rejection and infection. It is of paramount importance to
immunosuppress the patient to minimise the risk of allograft
rejection, without over-immunosuppressing and thereby
increasing susceptibility to opportunistic infection. For this
reason, cyclosporin-A blood levels are regularly monitored post-
operatively. Side effects include renal failure, hypertension,
hyperkalaemia, hirsutism, gum hypertrophy and increased
susceptibility to opportunistic infection and to lympho-
proliferative disorders. Tacrolimus acts in a similar way to
cyclosporin-A although it may be a more potent immunosup-
pressive agent. Although its side effect profile is similar, diabetes
mellitus can be a complication. Azathioprine is an antimetabolite
whose major side effects include bone marrow suppression and
hepatic cholestasis. Occasionally pancreatitis can occur. Some
patients who are intolerant of azathioprine are prescribed
mycophenolate mofetil (which is less likely to cause bone
marrow suppression) or cyclophosphamide. At the present time
the precise role of tacrolimus and mycophenolate in post-cardiac